Pesticide compositions and method

ABSTRACT

Toxicant, especially pesticide compositions, having lowered dermal toxicity are provided. The compositions include a lipophilic-pesticide, a nonionic surfactant and a dry inert diluent carrier. Methods for reducing the dermal toxicity of lipophilic toxicants, especially pesticides are provided, as well as methods for controlling insect pests using the disclosed compositions.

This application is a division of application Ser. No. 07/232,193, filedAug. 15, 1988, and now U.S. Pat. No. 4,994,261.

FIELD OF THE INVENTION

The invention relates to dermally toxic pesticide compositionsconsisting of the pesticide and a dry, inert diluent carrier, that havebeen additionally safened for handling by addition thereto of a nonionicsurfactant having an HLB of from about 17 to about 20.

BACKGROUND OF THE INVENTION

A wide variety of pesticides are commonly used in agronomic andhorticultural pursuits. As used herein the term "pesticide" means anychemical compound or composition which displays biological activity inan agricultural field site or at any locus where control of biologicalgrowth is desired. The biological activity or control contemplatedherein includes all forms of growth modification, ranging fromregulation and retardation to killing, and extends to all forms of plantand animal life found in an agricultural environment during some timeduring the pest's life cycle. Pesticides within this invention includeanti-foulants, plant growth regulants, soil fumigants, molluscicides,insecticides, herbicides, fungicides, rodenticides, nematocides,algicides, predator control agents, and insect and animal repellents.Additional biologically active compounds can also be present inadmixture with the primary ingredient, such as synergists, antidotes,fertilizers, soil life extenders, and additional pesticides.

The term "biologically effective amount" is used herein to denote anyquantity of pesticide or pesticide composition, which when applied to anagricultural site in any conventional manner causes the occurrence ofone or more of the biological effects mentioned above. As furtherexplained in the latter portion of this specification, the quantity ofpesticide applied in a given situation depend on the pesticide itself,on the type of biological activity inherent in the pesticide, and thedegree of such activity sought to be achieved. The selection of theproper quantity to be applied, however, is within the expertise of oneskilled in the art.

Some pesticides, such as the chlorinated hydrocarbon carbamateinsecticides and the organophosphorus pesticide compounds, includingphosphonate, organophosphate and organothiophosphate compounds present aproblem of dermal toxicity to persons handling these substances.

If handled carelessly, improperly or in disregard of directions, thepesticide, depending upon its toxicity, may present a hazard to thosehandling the pesticide whether in packaging it for sale, handling it forshipment, mixing it for field application or applying it in the field.The toxicity of the pesticide will vary depending upon a number offactors, including the inherent toxicity of the pesticide substance atits site of biological action. Various physical properties of thepesticide including the hydrophilic-lipophilic balance of the pesticideaffect the adsorption to and absorption by various tissues of the personhandling the pesticide compound, and thus affect the toxicity of thecompound to the person handling it.

Thus, it is desirable to develop formulations for these pesticidecompounds that reduce the dermal toxicity of the compounds to personshandling them yet still preserve the pesticidal effectiveness of thecompounds as applied to the pest or the locus where the pest may befound.

SUMMARY OF THE INVENTION

There has now been discovered a pesticidal composition that maintainshigh biological effectiveness against pests when used in the field andhas reduced dermal toxicity.

The compositions comprise a biologically effective amount of a dermallytoxic pesticide, a nonionic surfactant having an HLB of from about 17 toabout 20 and a dry inert diluent carrier.

More particularly, the compositions comprise

(a) a biologically effective amount of a dermally toxic pesticide;

(b) a dinonyl phenol ethoxylate surfactant; and

(c) a dry inert diluent clay carrier, in granular form.

Dermal toxicity includes systemic toxic effects that occur in an animalor human as a result of dermal contact with a toxic substance for adefined period of time. Dermal toxicity may be defined as the LD-50(lethal dose to 50% of the animals in a test group) caused by a 24 hourexposure to a toxic substance.

Pesticides of the composition disclosed herein include dermally toxicorganophosphorus, pyrethroids, phosphonate and thiophosphonatecompounds. The following are examples of such compounds, followed inparenthesis by their common names, where available:

S-tert-butylthiomethyl O,O-diethyl phosphorodithioate (terbufos)

O,O-diethyl-O-4-methylsulphinylphenyl phosphorothioate (fensulfothion)

O,O-diethyl O-2-isopropyl-6-methylpyridimidin-4-yl phosphorothioate(diazinon)

O,O-diethyl S-2-ethylthioethyl phosphorodithioate (disulfoton)

S-chloromethyl O,O-diethyl phosphorodithioate (chlormephos)

O-ethyl S,S-dipropyl phosphorodithioate (ethoprophos)

O,O-diethyl S-ethylthiomethyl phosphorodithioate (phorate)

O-(4-bromo-2-chlorophenyl) O-ethyl S-propyl phosphorodithioate(prophenofos)

S-1,2-di(ethoxycarbonyl)ethyl O,O-dimethyl phosphorodithioate(malathion)

O,O,O',O'-tetraethyl S,S"-methylene di(phosphorodithioate) (ethion)

O-(4-bromo-2,5-dichlorophenyl) O,O-diethyl phosphorothioate(bromophos-ethyl)

S-4-chlorophenylthiomethyl O,O-diethyl phosphorodithioate(carbophenothion)

2-chloro-1-(2,4-dichlorophenyl)vinyl diethyl phosphate(chlorophenvinphos)

O-2,5-dichloro-4-(methylthio) phenyl O,O-diethyl phosphorodithioate(chlorthiophos)

O-4-cyanophenyl O,O-dimethyl phosphorothioate (cyanophos)

O,O-dimethyl O-2-methylthioethyl phosphorothioate (demiphion)

O,O-diethyl O-2-ethylthioethyl phosphorothioate (demeton)

O-2,4-dichlorophenyl O,O-diethyl phosphorothioate (dichlorofenthion)

O-2,4-dichlorophenyl O-ethyl phenylphosphonothioate (EPBP)

O,O-diethyl O-5-phenylisoxazol-3-yl phosphorothioate (isoxathion)

1,3-di(methoxycarbonyl)-1-propen-2-yl dimethyl phosphate

1,4-dioxan-2,3-diyl S,S-di(o,O-diethyl phosphorothioate (dioxathion)

O,O-dimethyl-O-4-nitro-m-tolyl phosphorothioate (fenitrothion)

O,O-dimethyl O-4-methylthio-m-tolyl phosphorothioate (fenthion)

O-(5-chloro-1-isopropyl-1,2,4-triazol-3-yl) O,O-diethyl phosphorothioate(isazophos)

S-2-isopropylthioethyl O,O-dimethyl phosphorodithioate (isothioate)

4-(methylthio)phenyl dipropyl phosphate (propaphos)

1,2-dibromo-2,2-dichloroethyl dimethyl phosphate (naled)

O,O-diethyl α-cyanobenzylideneamino-oxyphosphonothioate (phoxim)

O,O-diethyl O-4-nitrophenyl phosphorothioate (parathion)

O-2-diethylamino-6-methylpyrimidin-4-yl O,O-diethyl phosphorothioate(pirimiphos-ethyl)

O-2-diethylamino-6-methylpyrimidin-4-yl O,O-dimethyl phosphorothioate(pirimiphos-methyl)

O,O,O',O'-tetraethyldithiopyrophosphate (sulfotep)

O,O,O',O'-tetramethyl O,O'-thiodi-p-phenylene diphosphorothioate(temephos)

S-2-ethylthioethyl O,O-dimethyl phosphorodithioate (thiometon)

O,O-diethyl O-1-phenyl-1,2,4-triazol-3-yl phosphorothioate (triazophos)

O-ethyl O-2,4,5-trichlorophenyl ethylphosphonothioate (trichloronate)

(±)-3-allyl-2-methyl-4-oxocyclopent-2-enyl (±)-cis,trans-chrysanthemate(allethrin)

(±)-3-allyl-2-methyl-4-oxocyclopent-2-enyl (±)-trans-chrysanthemate(bioallethrin)

3-phenoxybenzyl (±)-cis,trans-chrysanthemate (phenothrin) pyrethrins

2-(2-butoxyethoxy)ethyl thiocyanate

isobornyl thiocyanoacetate (terpinyl thiocyanoacetate)

carbon disulfide

2-(4-tert-butylphenoxy)cyclohexyl prop-2-ynyl sulphite (propargite)

4,6-dinitro-6-octylphenyl crotonates (dinocap)

ethyl 4,4'-dichlorobenzilate (chlorobenzilate)

S,S,S-tributyl phosphorotrithioate

tributyl phosphorotrithioite (merphos)

copper naphthenates

5-ethoxy-3-trichloromethyl-1,2,4-thiadiazole (etridiazole)

O-ethyl S,S-diphenyl phosphorodithioate (edifenphos)

6-butoxycarbonyl-2,3-dihydro-2,2-dimethylpyran-4-one (butopyronoxyl)

N,N-diethyl-m-toluamide (deet)

dibutyl phthalate

dibutyl succinate

1,5a,6,9,9a,9b-hexahydro-4a(4H)-dibenzofurancarboxaldehyde

dipropyl pyridine-2,5-dicarboxylate

Of the many different types of pesticides useful in the presentcomposition, certain classes are preferred. One preferred class is thatof organosphosphorus compounds, particularly those of the formula:##STR1## in which X is oxygen or sulfur; and R, R₁ and R₂ areindependently selected from the group consisting of C₁ -C₆ alkyl, C₁ -C₆alkoxy, C₁ -C₆ alkylthio, C₂ -C₆ alkenyl, C₂ -C₆ alkenoxy, C₂ -C₆alkenylthio, phenyl, phenoxy, phenylthio, C₇ -C₉ phenylalkyl, C₇ -C₉phenylalkoxy, and C₇ -C₉ phenylalkylthio, each member of such groupoptionally substituted with up to three substituents selected fromhalogen, C₁ -C₄ alkyl, C₁ -C₄ alkoxy, cyano, and nitro.

The terms "alkyl," "alkoxy," etc., are intended to include bothstraight-chain and branched-chain groups, and all carbon atoms rangesare inclusive. More preferred organophosphorus compounds are those inwhich X is sulfur, and R, R₁ and R₂ are independently C₁ -C₄ alkoxy orphenoxy, the phenyl ring optionally substituted with up to three groupsselected from C₁ -C₃ alkyl, nitro, cyano, and halogen. Highly preferredare those in which X is sulfur, R is C₁ -C₄ alkoxy, R₁ is C₁ -C₄ alkoxy,and R₂ is phenoxy substituted with up to three substituents selectedfrom C₁ -C₃ alkyl and nitro.

Specific preferred pesticide compounds includeS-tert-butylthiomethyl-O,O-diethylphosphorodithioate andO,O-diethyl-S-ethylthiomethylphosphorothioate.

The most highly preferred are compounds of the general formula: ##STR2##wherein R₃ and R₄ are selected from the group consisting of methyl andethyl and Y is selected from the group consisting of hydrogen and alkylgroups having up to 4 carbon atoms.

The most highly preferred pesticide compounds serving as the activeingredients in the compositions of this invention are those described inU.S. Pat. No. 2,988,474, with the most preferred compound beingo-ethyl-S-phenylethyl phosphonodithioate, sold under the tradenameDyfonate® by Stauffer Chemical Company.

Surfactants which are suitable for use in the compositions are nonionicand have an HLB (hydrophilic-lipophilic balance) of from about 17 toabout 20.

The most preferred surfactant is manufactured under the tradenameIgepal® DM 970 by the GAF Corporation, and under different tradenames byvarious companies, and is a dinonyl phenyl-150 mole ethoxylate. It hasan HLB of 19.0.

The inclusion of the nonionic surfactant in this formulation serves tochemically stablize the organophosphorus or other active pesticidecompound on the clay granules, and also has the effect of reducing thedermal toxicity of the organophosphorus/clay granule formulation.

Other suitable surfactants of the general composition are, for example,alkyl and dialkylphenoxy poly(ethyleneoxy) ethanols. Suitablesurfactants of the above-mentioned HLB range are exemplified bysurfactants of the following structural formula ##STR3## wherein n is 1or 2.

Further examples of appropriate surfactants according to the inventionare summarized in Table I.

                  TABLE I                                                         ______________________________________                                        HLB   Commercial Name                                                                              Structure                                                ______________________________________                                        17.9  Myrj 53        polyoxyethylene (50) stearate                            18.0  Etocas 100     ethoxylated (100) castor oil                             18.0  Lantrol AWS    alkoxylated lanolin oil                                  18.0  Veronic L167   ethoxylated coco mono-glyceride                          18.1  Alcasurf CO200 ethoxylated castor oil                                   18.1  Chemmax CO-200/50                                                                            ethoxylated castor oil                                   18.1  Pegosperse CO200                                                                             POE 200, castor oil                                      18.1  Veronic Li48   ethoxylated mono and diglyceride                         18.0  Tergitol 15-S-50                                                                             secondary alcohol PEG ether                              18.3  Kessco polyethylene                                                                          esters, PEG 4000 monoleate                                     glycol                                                                  18.8  Brig 700       polyethylene 100 stearyl ether                           18.8  Kessco PEG esters                                                                            PEG monostearate                                         18.5  Pluronic L-35                                                           17.0  Pluronic P-65                                                           ______________________________________                                    

Preferred clays for use as the inert diluents in the compositions ofthis invention are those from the attapulgite group and those from themontmorillonoid group. The attapulgite clays have the prototype formulaMg₅ Si₈ O₂₀ (OH)₂₈ H₂ O and those of the montmorillonoid group have theprototype formula Al₂ (Si₄ O₁₀)(OH)₂.

The attapulgite clays are most effective for use in the compositions ofthe invention as inert diluent carriers.

Both of these types of clays are well known to those skilled in the artand are described in the Handbook of Insecticide Dust Diluents andCarriers, by T. C. Watkins and L. B. Norton, Dorland Books, Caldwell,N.J. (1955).

Other conventional diluent carriers can be used, but the clays arepreferable.

The active ingredients (pesticide and surfactant) are sprayed onto theclays and blended to yield formulations with the active componentdistributed uniformly throughout the mass. The granular compositions ofthis invention are most useful in a size range of from 10-60, preferably18-48 mesh, U.S. Sieve Series Number.

Accordingly, the preferred composition of this invention comprises

(a) from about 1 to about 45 percent by weight of a biologicallyeffective amount of an organophosphorus compound of the formula ##STR4##wherein R₃ and R₄ are selected from the group consisting of methyl andethyl and Y is selected from the group consisting of hydrogen and alkylgroups having up to 4 carbon atoms.

(b) from about 0.1 to about 10 percent by weight of dinonyl phenol 150mole ethoxylate; and

(c) from about 50 to about 98 percent by weight clay granules.

While the formulation set forth above is described in terms of anorganophosphorus compound such as described in U.S. Pat. No. 2,988,474,it is also contemplated that other hydrophobic pesticides--clay granuleformulations can be dermally safened using this class of surfactants asdescribed herein.

Formulations of the type described herein are set forth below.

    ______________________________________                                        Counter ® *                                                                           15%       Thimet ® **                                                                           20%                                         attapulgite 80%       attapulgite 75%                                         clay granules         clay granules                                           Igepal DM 970                                                                              5%       Igepal DM 970                                                                              5%                                                     100%                  100%                                        Dyfonate ®                                                                            15%       Dyfonate ®                                                                            20%                                         attapulgite 80%       attapulgite clay                                                                          75%                                         clay granules         granules                                                Igepal DM 970                                                                              5%       Igepal DM 970                                                                              5%                                                     100%                  100%                                        ______________________________________                                         *S-tert-butylthiomethyl O,Odiethyl phosphorodithioate                         **O,Odiethyl Sethylthiomethylphosphorodithioate                          

The Igepal DM970 has the structural formula ##STR5##

The pesticide formulation is normally prepared by taking a quantity ofDyfonate® and mixing therewith the desired quantity of Igepal DM 970 andapplying that mixture to clay granules, and mixing the clay granuleswith the active ingredient thoroughly. A typical process is as follows.

EXAMPLE 1

Five grams (5 g) of Igepal DM970 was dissolved in a solution of 15.82 gof Dyfonate® technical material (95% active ingredient) in a water bathheated between 55°-75° C. This solution was then added with a pipette toa quantity (79.18 g) of clay granules in a rotating beaker. The tumblingwas continued for approximately one hour after the addition of theactive ingredient to effect mixing of all of the components.

The pesticide compositions according to the invention may have variousamounts of pesticide, surfactant and dry inert diluent carrier.

The amount of pesticide compound include in the pesticidal granulecomposition depends on the absorption capacity of the inert carrier andthe spreading efficacy of the application equipment. In general, thepesticide may comprise from 1% to about 45% of the composition on aweight basis, preferably about 15%.

Expressed as a weight percent of the whole composition, the surfactantmay range between about 0.1% and about 10% with a preferred range ofbetween 1% and 6% and an optimal range of between 2% and 5%, dependingupon the exact composition of the surfactant.

The amount of dry inert diluent carrier in pesticidal compositions mayvary between 50% and about 98%, most preferably about 80%.

The invention will be better understood with respect to the followingexamples which are intended by the inventors to be exemplary only andnon-limiting.

The reduction in dermal toxicity achieved by the use of the compositionsof the invention is demonstrated in accordance with the followingexamples.

In conducting the dermal toxicity tests in Example II, a comparison wasmade between two formulations: one of these formulations containing theIgepal DM 970 nonionic surfactant, and the other containing aconventional chemical stabilizer, dipropylene glycol. The dermaltoxicity was measured in accordance with the following technique.

EXAMPLE II Dermal Toxicity

Acute dermal toxicity was determined in accordance with theEnvironmental Protection Agency's Proposed Guidelines for RegisteringPesticides in the U.S.; Hazard Evaluation: Humans and Domestic Animals,Fed. Reg. 43:163, 37336-37402 (Aug. 22, 1978).

Albino rabbits (Stauffland White strain, Phillips Rabbitry, Soquel,Calif.) were housed in temperature controlled animal rooms (65°-70° F.),two to a cage in suspended steel cages (24"×16.5"×14"). Feed (SpecialMixture, Gunter Bros., Morgan Hill, Calif.) and water were provided adlibitum.

Prior to treatment, the rabbits were randomly selected and individuallyidentified using numbered ear tags. The day before treatment the skinareas to be treated were closely clipped and the rabbits were fastedovernight with water available.

The first dose tested was 501 mg/kg in 10 rabbits, 5 males and 5females. Doses were thereafter selected at logarithmically spacedintervals. The levels selected produced at least three test groups withmortality rates between 10% and 90% and permitted calculation of theLD₅₀ (abraded skin and/or intact skin) of males and females with a 95%confidence interval of 20% or less. At least three dose levels andcontrols were tested.

Four male and four female rabbits were used for each succeeding doselevel. In some of the tests, half of the rabbits at each dose level werefurther prepared by making epidermal abrasions with a needle in across-hatch manner over the entire exposure area. The abrasions weresufficiently deep to penetrate the stratum corneum, but not the dermis.A single application of the composition was applied neat to the dosesite. The composition was held in contact with the skin by anon-absorbent binder. To insure the integrity of the binder an outerwrapping of gauze was applied. At the end of the 24 hour exposureperiod, the wrappings were removed and the skin wiped and/or washed toremove any remaining test substance. The animals were then wrapped withfresh gauze which was left in place for 72 hours.

Four rabbits (two of each sex) were sham-treated by wrapping each in asimilar manner.

Animals were observed for at least 14 days after dosing or until allsigns of reversible toxicity in survivors subsided, whichever occurredlater.

Observation for clinical signs and mortality were recorded frequentlythe first day, and early morning and late afternoon thereafter. Theanimals were observed once a day during weekends and holidays. Allclinical signs were recorded for the onset, duration and severity.Rabbits were weighed on days 0 (prior to treatment), 7, 14 or at death,with the mean body weight calculated for each day.

The acute dermal toxicity in these tests was found to be unaffected byprior abrasion of the skin of the test animals. The results of thesetests are reported in Table II.

                  TABLE II                                                        ______________________________________                                        Determination of LD.sub.50 According to                                       the Method of Litchfield and Wilcoxon                                         Route: Dermal  Species: Rabbit  Sex: Both                                             Formulation   Dermal LD.sub.50                                        ______________________________________                                        1.    15%     Dyfonate ®  254 (163-394)*                                        5%      dipropylene glycol                                                    80%     attapulgite clay granules                                             100%                                                                    2.    15%     Dyfonate ®  453 (307-667)*                                        5%      Igepal DM 970                                                         80%     attapulgite clay granules                                             100%                                                                    ______________________________________                                         *Values in parentheses are 95% confidence limits.                             LD.sub.50 is measured in mg of composition per kg of body weight.        

It can be seen by comparing the application of the two formulationsabove that the pesticide formulation containing the Dyfonate®, Igepal DM970 and attapulgite clay was about one-half as dermally toxic as was thecomparison formulation containing Dyfonate®, dipropylene glycol andattapulgite clay.

EXAMPLE III

Similar tests were conducted with additional formulations wherein theactive ingredient was varied by replacing the Dyfonate® pesticide withother pesticides of the organophosphorus-type. The results of thesetests, along with the formulations, are set forth in Table III below.

                  TABLE III                                                       ______________________________________                                        Determination of LD.sub.50 According to                                       the Method of Litchfield and Wilcoxon                                         Route: Dermal  Species: Rabbit  Sex: Both                                              Formulation Dermal LD.sub.50                                         ______________________________________                                        1.     20%     Thimet ®  162 (136-182)*                                          5%      dipropylene glycol                                                    75%     attapulgite clay                                                      100%                                                                   2.     20%     Thimet ®  231 (208-258)*                                          5%      Igepal DM 970                                                         75%     attapulgite clay                                                      100%                                                                   3.     15%     Counter ® 23.5 (19.7-28.1)                                        5%      dipropylene glycol                                                    80%     attapulgite clay                                                      100%                                                                   4.     15%     Counter ® 42.9 (36.7-50.3)                                        5%      Igepal DM 970                                                         80%     attapulgite clay                                                      100%                                                                   ______________________________________                                         *Values in parentheses are 95% confidence limits.                             LD.sub.50 is measured in mg of composition per kg of body weight.        

Again it will be seen that the substitution of the surfactant Igepal DM970 for dipropylene glycol was effective in reducing the dermal toxicityof the formulation by a factor of about 2.

Insecticidal Effectiveness

The insecticidal effectiveness of the composition was tested in thefollowing manner:

One cubic centimeter (cc) of Western spotted cucumber beetle larvae(Diabrotica undecimpunctata) supplied by Mannerheim)] containing about7,000 eggs was diluted to a final concentration of 250 eggs/cc bysuspending 0.5 cc of undiluted eggs in 14 cc of water containing 0.2%Dacagin (Diamond Alkali Co.). Eggs may be stored in this suspension for5 days at 5° C. without significant loss of viability.

Ten grams (10 g) of moist "Supersoil" (Wonderline, Rod McLellan Co., SanFrancisco, Calif.) were placed in a one ounce clear plastic cup(Thunderbird Container Corporation, El Paso, Tex.). The test materialwas dissolved in acetone or an appropriate solvent. A 0.05 milliliter(ml) aliquot of the test sample that had been diluted to the desiredconcentration was added to the soil. The cup was capped and the soil wasmixed on a Vari-Whirl mixer for approximately 15 seconds. An indentationwas made on the surface of the soil and 0.2 cc of the egg suspension wasadded. The eggs were covered with soil and maintained at roomtemperature (approximately 70° F.). Four days later a section of Romainelettuce leaf was placed in the treated cups. One week later the cupswere examined for live larvae.

Test concentrations range from 10 ppm down to that at whichapproximately 50% mortality occurs.

There were two test compositions used to compare the insecticidaleffectiveness of the compositions of this invention. The firstcomposition (1) formulated in accordance with the compositions of theinvention contained 15% Dyfonate®, 5% Igepal DM 970 and 80% attapulgite,and the second (2) contained 20% Dyfonate®, 5% dipropylene glycol and75% attapulgite. The results of these tests are set forth in Table IVbelow.

                  TABLE IV                                                        ______________________________________                                                    Diabrotica LC.sub.50 Value (ppm)                                  ______________________________________                                        Composition No. 1                                                                           0.4                                                             Composition No. 2                                                                           0.4                                                             ______________________________________                                    

As can be seen from the results set forth above, the LC₅₀ value againstDiabrotica of the composition of the invention was the same as that of asimilar composition containing the conventional chemical stabilizer,dipropylene glycol. This demonstrates that the substitution of theIgepal DM 970 for dipropylene glycol does not adversely effect thebiological effectiveness of the active ingredient.

It will be readily apparent to those skilled in the art that thecompositions of the invention offer markedly reduced dermal toxicitywithout significantly reducing the biological effectiveness of thepesticidal compound used in the composition.

What is claimed is:
 1. A granular pyrethroid pesticide composition thathas been safened for handling comprising:(a) from about 1 to about 45percent by weight of a dermally toxic pyrethroid pesticide compound; (b)from about 0.1 to about 10 percent by weight of a nonionic surfactant ofthe formula ##STR6## wherein n is 1 or 2; and (c) from about 50 to about98 percent by weight of a dry inert diluent carrier.
 2. The compositionof claim 1 wherein said surfactant is dinonyl phenol-150 moleethoxylate.
 3. The composition of claim 1 wherein the dry inert diluentcarrier is an attapulgite clay and comprises between 50% and about 98%on a weight basis of said composition.
 4. The method of reducing dermaltoxicity to a mammal exposed to a granular, dermally toxic pyrethroidcompound comprising the steps of adding to said dermally toxicpyrethroid compound an amount of a nonionic surfactant of the formula##STR7## wherein n is 1 or 2, sufficient to reduce the dermal toxicityof said dermally toxic pyrethroid compound.